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United States · US · US:59208-002_24b2e848-505d-3cf9-e063-6394a90a16d7
CICLOFERON
UNIISPLATC D08AJ
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLaboratorios Liomont, S.A. de C.V.
CountryUS (United States)
ATC codeD08AJ
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1159208002041 TUBE in 1 CARTON (59208-002-04) / 4 g in 1 TUBE
- ndc1159208002051 TUBE in 1 CONTAINER (59208-002-05) / 4 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
F5UM2KM3W7
BENZALKONIUM CHLORIDE
RxCUI 1379
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "F5UM2KM3W7",
"rxcui": "1379",
"inchikey": null,
"display_name": "BENZALKONIUM CHLORIDE",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"89081ef8-9721-a476-e053-2995a90ae0de": {
"match": "brand_token",
"title": "CICLOFERON (BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE) GEL [LABORATORIOS LIOMONT, S.A. DE C.V.]",
"spl_version": "2",
"published_date": "2024-10-21"
}
},
"productid": "59208-002_24b2e848-505d-3cf9-e063-6394a90a16d7",
"productndc": "59208-002",
"dosage_form": "GEL",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZALKONIUM CHLORIDE; LIDOCAINE HYDROCHLORIDE",
"proprietary_name": "CICLOFERON",
"active_ingred_unit": "mg/g; mg/g",
"application_number": "M003",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "benzalkonium chloride and lidocaine hydrochloride",
"start_marketing_date": "20190501",
"active_numerator_strength": "1.3; 20"
}Related drugs
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